Synthesis, X-ray crystal structure, and electrochemistry of copper(II) complexes of a new tridentate unsymmetrical Schiff base ligand and its hydrolytically rearranged isomer

A new unsymmetrical Schiff base ligand HL1, HBacabza, and its copper(II) complexes [Cu2L12(OAc)2] (1) and [Cu2L22(N3)2]·2H2O (2) with HBacabza = 3-(2-aminobenzylimino)-1-phenylbutan-1-one as HL1 and its hydrolytically rearranged isomer 3-(2-aminomethylphenyleneimino)-1-phenylbutan-1-one as HL2, have been synthesized and characterized by elemental analyses and spectroscopic methods. The rearrangement of HL1 to HL2 occurs in a hydrolysis-recondensation process in the reaction of HL1 with Cu(ClO4)2·6H2O and NaN3. The crystal structures of the ligand and its complexes have been determined by single crystal X-ray diffraction. The deprotonated Bacabza− coordinates to the metal center as a tridentate ligand. The acetate anion coordinates through one oxygen atom in complex 1 leading to a mono-atomic acetate oxygen-bridging dimeric copper(II) complex. Similarly, the azide anion coordinates through one nitrogen atom in complex 2 leading to a mono-atomic azide nitrogen-bridging dimeric copper(II) complex. The copper(II) ions adopt a distorted square pyramidal (4 + 1) coordination in these two complexes. The cyclic voltammetric studies of these complexes in N,N-dimethylformamide indicate that the reduction process corresponding to CuII/CuI is electrochemically irreversible in complex 1, presumably due to the structural changes during the course of redox reaction, and quasi-reversible in complex 2.

A new unsymmetrical N2O Schiff base ligand HL1, formed by the condensation of benzoylacetone and 2-aminobenzylamine, and its copper complex [Cu2L12(OAc)2] (1) and the copper azide complex of its hydrolytically rearranged isomer [Cu2L22(N3)2]·2H2O (2) have been synthesized and fully characterized. The X-ray crystal structures of HL1, 1, and 2 have been determined. Spectral and electrochemical studies are also reported.Figure optionsDownload as PowerPoint slideHighlights
► A new unsymmetrical N2O Schiff base, HL1, has been synthesized and characterized.
► The mono-atomic acetate O-bridgeddimeric Cu(II) complex of L1 has been prepared.
► The CuII and anion promoted hydrolytic rearrangement of L1 to L2 is documented.
► The μ-1,1 (EO) azide dimeric Cu(II) complex of L2 has been synthesized.
► X-ray structure and cyclic voltammetry of the two complexes have been studied.